NM_001370259.2(MEN1):c.*104C>T AND Hyperparathyroidism
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000398139.6
Allele description [Variation Report for NM_001370259.2(MEN1):c.*104C>T]
NM_001370259.2(MEN1):c.*104C>T
Condition(s)
- Name:
- Hyperparathyroidism
- Identifiers:
- MONDO: MONDO:0001741; MedGen: C0020502; Human Phenotype Ontology: HP:0000843
-
Profile neighbors for GEO Profiles (Select 23493963) (200)
GEO Profiles
-
[Candida] auris isolate MIC-44 internal transcribed spacer 1, partial sequence; ...
[Candida] auris isolate MIC-44 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequencegi|1942249246|gb|MW358015.1|Nucleotide
-
cytochrome oxidase subunit 1 (mitochondrion) [Schizosaccharomyces pombe]
cytochrome oxidase subunit 1 (mitochondrion) [Schizosaccharomyces pombe]gi|1707764602|gb|QDP17274.1|Protein
-
Homo sapiens cDNA, FLJ95286
Homo sapiens cDNA, FLJ95286gi|164698226|dbj|AK314479.1|Nucleotide
-
txid2078957[Organism:noexp] (19676)
Identical Protein Groups
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Apr 9, 2023